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富马酸替诺福韦艾拉酚胺的治疗会恶化感染 HIV 患者的血脂水平,与富马酸替诺福韦二吡呋酯联合艾维雷韦、考比司他和恩曲他滨的治疗相比。

Treatment with tenofovir alafenamide fumarate worsens the lipid profile of HIV-infected patients versus treatment with tenofovir disoproxil fumarate, each coformulated with elvitegravir, cobicistat, and emtricitabine.

机构信息

Division of Clinical Virology, Biomedical Research Institute of A Coruña (INIBIC)-Universitary Hospital of A Coruña (CHUAC), SERGAS, University of A Coruña (UDC), A Coruña, Spain.

Service of Pharmacy, Universitary Hospital of A Coruña (CHUAC), SERGAS, A Coruña, Spain.

出版信息

Basic Clin Pharmacol Toxicol. 2019 Apr;124(4):479-490. doi: 10.1111/bcpt.13161. Epub 2018 Dec 7.

DOI:10.1111/bcpt.13161
PMID:30388308
Abstract

Two elvitegravir/cobicistat-based therapies combined with emtricitabine/tenofovir disoproxil fumarate (EVG/c/FTC/TDF) or emtricitabine/tenofovir alafenamide fumarate (EVG/c/FTC/TAF) are currently available for HIV patients. This study evaluated the modifications in the lipid profile of patients who received these treatments in the last three years at our institution. A retrospective observational study in HIV-infected patients who received EVG/c/FTC/TDF or EVG/c/FTC/TAF from January 2015 to January 2018 at a reference hospital in northwestern Spain was carried out. Epidemiological, clinical and immunovirological data were recorded. A statistical analysis was performed using SPSS software. A total of 384 EVG/c-based therapies were initiated during the study period, 151 EVG/c/FTC/TDF and 233 EVG/c/FTC/TAF. A significantly negative influence in all the lipid profile parameters in experienced patients and total cholesterol (TC), and LDL-C in naïve patients were observed after 48 weeks of treatment with EVG/c/FTC/TAF, while these parameters remained stable in the EVG/c/FTC/TDF group. During follow-up, a greater proportion of patients had lipid levels above the normal range (63.1% TC, 56.2% LDL-C) and new lipid-modifying drugs were prescribed (11.9%) in the EVG/c/FTC/TAF group. The number of cardiovascular risk factors (OR 1.66 [95% CI 1.01-2.72]; P = 0.043) was recognised as an independent predictor of lipid-lowering prescription for patients treated with both EVG/c/FTC/TDF and EVG/c/FTC/TAF. For patients treated with EVG/c/FTC/TAF, the mean total cholesterol to HDL ratio in the first 48 weeks of the study treatment was associated with a higher likelihood of lipid-lowering prescription in multivariate analysis (OR 1.6 [95% CI 1.12-2.52]; P = 0.011). Significant changes in lipid profile have been observed in patients who have received EVG/c/FTC/TAF. It was necessary to prescribe almost twice the number of lipid-lowering drugs to patients who received EVG/c/FTC/TAF (11.9%) vs EVG/c/FTC/TDF (4.7%).

摘要

两种基于艾维雷格/考比司他的疗法联合恩曲他滨/替诺福韦富马酸酯(EVG/c/FTC/TDF)或恩曲他滨/丙酚替诺福韦(EVG/c/FTC/TAF)目前可用于治疗 HIV 患者。本研究评估了过去三年在我院接受这些治疗的患者脂质谱的变化。在西班牙西北部一家参考医院进行了一项回顾性观察性研究,研究对象为 2015 年 1 月至 2018 年 1 月期间接受 EVG/c/FTC/TDF 或 EVG/c/FTC/TAF 的 HIV 感染患者。记录了流行病学、临床和免疫病毒学数据。使用 SPSS 软件进行了统计分析。在研究期间,共启动了 384 次 EVG/c 为基础的治疗,其中 151 次为 EVG/c/FTC/TDF,233 次为 EVG/c/FTC/TAF。接受 EVG/c/FTC/TAF 治疗 48 周后,经验丰富的患者所有脂质谱参数和总胆固醇(TC)及 LDL-C 显著负向变化,而 EVG/c/FTC/TDF 组这些参数保持稳定。在随访期间,EVG/c/FTC/TAF 组有更多的患者血脂水平超过正常范围(TC63.1%,LDL-C56.2%)和新的调脂药物(11.9%)处方。心血管危险因素数量(OR1.66[95%CI1.01-2.72];P=0.043)被认为是患者同时接受 EVG/c/FTC/TDF 和 EVG/c/FTC/TAF 治疗时调脂药物处方的独立预测因素。对于接受 EVG/c/FTC/TAF 治疗的患者,在研究治疗的前 48 周,总胆固醇与高密度脂蛋白比值的平均值与多变量分析中调脂药物处方的可能性较高相关(OR1.6[95%CI1.12-2.52];P=0.011)。接受 EVG/c/FTC/TAF 治疗的患者脂质谱发生了显著变化。与接受 EVG/c/FTC/TDF(4.7%)的患者相比,接受 EVG/c/FTC/TAF(11.9%)的患者需要开具近两倍数量的调脂药物。

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